Year 9 Science Unit 1 · Disease Lesson 7 of 20 45 min SC5-DIS-07

The Third Line — Lymphocytes

While inflammation and phagocytes fight every invader the same way, your third line of defence is different. It learns, remembers, and targets specific enemies with precision. B cells, T cells, and antibodies form the most sophisticated defence system in the known universe — and it lives inside you.

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Think First

Before You Begin

Imagine you catch a disease, recover, and then encounter the same disease years later.

Write down your answers before reading on:

  • Why do you usually not get sick the second time?
  • What do you think your body remembers about the first infection?
  • Why do some diseases (like chickenpox) give lifelong immunity while others (like flu) do not?
Write your thinking in your book before reading on.

Work mode: Digital — answers typed below

Know

  • The components of the third line of defence: B cells, T cells, antibodies
  • How antigens trigger the specific immune response
  • The difference between the primary and secondary immune response

Understand

  • Why the third line is called "specific"
  • How memory cells enable faster future responses
  • The roles of B cells and T cells in immunity

Can Do

  • Explain how antibodies recognise and neutralise specific pathogens
  • Describe the primary and secondary immune responses
  • Compare the second and third lines of defence
Key Terms
Third line of defence The specific immune response involving lymphocytes (B cells and T cells) that targets particular pathogens.
Lymphocyte A type of white blood cell involved in the specific immune response: B cells produce antibodies; T cells kill infected cells.
B cell A lymphocyte that produces antibodies specific to a particular antigen.
T cell A lymphocyte that directly kills infected body cells or helps coordinate the immune response.
Antibody A protein produced by B cells that binds to a specific antigen and helps neutralise or destroy the pathogen.
Antigen A substance on the surface of a pathogen that triggers an immune response.
Memory cell A long-lived lymphocyte that remains after an infection and enables a faster response if the same pathogen is encountered again.
1

Antigens and Specificity

How the immune system recognises enemies

Inflammation

Inflammation

Every pathogen has unique molecules on its surface called antigens. Think of antigens as identity badges that tell the immune system exactly what it is facing.

The third line of defence is specific because lymphocytes produce responses tailored to particular antigens. Unlike the second line (which attacks all pathogens the same way), the third line creates customised weapons for each enemy.

When a pathogen enters the body, its antigens are detected by specialised cells called lymphocytes. There are two main types:

  • B cells — produce antibodies that bind to antigens
  • T cells — kill infected cells and coordinate the immune response

Each lymphocyte is programmed to recognise one specific antigen. Your body contains millions of different lymphocytes, each waiting for its matching antigen.

2

B Cells and Antibodies

The molecular weapons

When a B cell encounters its matching antigen, it becomes activated and multiplies rapidly. Most of these activated B cells become plasma cells that produce and release thousands of antibodies per second.

Antibodies are Y-shaped proteins that work like guided missiles:

  • Neutralisation: Antibodies bind to viruses and toxins, blocking them from entering cells
  • Opsonisation: Antibodies coat pathogens, making them easier for phagocytes to engulf
  • Clumping: Antibodies stick pathogens together, making them easier targets
  • Complement activation: Antibodies trigger complement proteins to destroy pathogens

Some activated B cells become memory B cells that live for years or decades. If the same pathogen returns, memory B cells enable a much faster and stronger antibody response.

3

T Cells — The Cellular Killers

Directly destroying infected cells

While B cells fight pathogens in body fluids, T cells attack infected body cells directly. There are two main types:

Helper T cells coordinate the immune response by:

  • Activating B cells to produce antibodies
  • Activating cytotoxic T cells to kill infected cells
  • Releasing chemical signals (cytokines) that recruit other immune cells

Cytotoxic T cells (killer T cells) directly destroy infected body cells by:

  • Recognising infected cells that display foreign antigens on their surface
  • Releasing toxic chemicals that punch holes in the infected cell
  • Triggering the infected cell to self-destruct (apoptosis)

T cells are especially important for fighting viruses, which hide inside body cells where antibodies cannot reach them.

4

Primary and Secondary Responses

Why immunity gets stronger

The first time your body encounters a pathogen, it mounts a primary immune response:

  • Takes 5-10 days to reach full strength
  • Produces relatively few antibodies
  • You may feel sick during this time

After the infection is cleared, memory B cells and memory T cells remain in the body. If the same pathogen is encountered again, the secondary immune response is dramatically different:

  • Starts within 1-3 days
  • Produces 100-1,000 times more antibodies
  • The pathogen is usually eliminated before you feel sick

This is why you typically get diseases like chickenpox only once — your secondary response is so fast and strong that the virus is destroyed before it can cause symptoms. However, some pathogens (like influenza) mutate their antigens, allowing them to evade existing memory cells.

Common Misconceptions

"Antibodies are cells." No — antibodies are proteins produced by B cells (which are cells). Antibodies circulate in blood and body fluids, binding to specific antigens.

"The third line of defence works immediately like the first and second lines." No — the specific immune response takes 5-10 days to develop fully during a primary infection. This is why you feel sick for several days before recovering.

trong>"Once you have antibodies against a disease, you are protected forever." Not always — protection duration varies by disease. Some pathogens (like influenza) mutate rapidly, making existing antibodies ineffective. Also, antibody levels can decline over time.

Australian Context

Australian Immunology Research

The Walter and Eliza Hall Institute (WEHI): Based in Melbourne, WEHI is Australia's oldest medical research institute and a world leader in immunology. WEHI scientists discovered how lymphocytes develop and function, and they continue to lead research on cancer immunotherapy, autoimmune diseases, and infectious disease immunity. Their work on apoptosis (programmed cell death) has transformed cancer treatment worldwide.

Immunology in Aboriginal health: Australian researchers study how the immune systems of Aboriginal and Torres Strait Islander people respond differently to certain infections. For example, Aboriginal Australians appear to have stronger innate immune responses but may have different patterns of adaptive immunity, which may explain why some infectious diseases present differently. This research helps develop more effective treatments and vaccines for Indigenous communities.

The Doherty Institute and T cells: During the COVID-19 pandemic, Melbourne's Doherty Institute conducted world-leading research on T cell responses to SARS-CoV-2. They found that T cells provided important protection even when antibody levels declined, informing vaccine strategies and public health policy in Australia and globally.

✍ Copy Into Your Books

Key Cells

  • B cells: produce antibodies specific to antigens
  • T cells: kill infected cells, coordinate response
  • Memory cells: enable faster future responses

Antibodies

  • Y-shaped proteins that bind to specific antigens
  • Neutralise pathogens, mark them for destruction
  • Produced by plasma cells (activated B cells)

Primary vs Secondary

  • Primary: 5-10 days, slower, you feel sick
  • Secondary: 1-3 days, 100-1000x stronger, usually no symptoms
Activity 1

Immune Response Sequence

Put the immune response in order.

1 Number the following events in the correct order: antibodies bind to pathogen, B cell activated, pathogen antigens detected, memory cells formed, plasma cells produce antibodies.
Answer in your book.
2 Explain why T cells are essential for fighting viral infections, using the concept of where viruses replicate in the body.
Answer in your book.
3 A person has memory B cells for measles but still catches influenza every few years. Explain why.
Answer in your book.
Activity 2

Antibody Design

Understand how antibodies match antigens.

1 Describe the "lock and key" relationship between antibodies and antigens. Why is this relationship essential for immune specificity?
Answer in your book.
2 If a pathogen mutates so its antigens change shape, what happens to existing antibodies and memory cells?
Answer in your book.
3 Research one Australian disease where understanding lymphocytes has led to better treatment.
Answer in your book.
Multiple Choice
Q

Test Your Understanding

RememberBand 3

1. Which cells produce antibodies?

AT cells
BPhagocytes
CB cells
DRed blood cells
RememberBand 3

2. What is an antigen?

AA cell that destroys pathogens
BA substance on a pathogen that triggers an immune response
CA type of antibody
DA chemical produced during fever
UnderstandBand 4

3. Why is the secondary immune response faster and stronger than the primary response?

ABecause the pathogen is weaker the second time
BBecause memory cells enable a quicker reaction
CBecause fever is higher
DBecause phagocytes work faster
UnderstandBand 4

4. T cells are especially important for fighting:

ABacterial infections
BFungal infections
CViral infections
DParasitic infections
RememberBand 3

5. Which of the following best describes the third line of defence?

ANon-specific and immediate
BSpecific and delayed
CPhysical barriers
DChemical barriers
Short Answer

Short Answer Questions

UnderstandBand 4

1. Compare the second and third lines of defence in terms of speed, specificity, and the cells involved. 4 MARKS

Answer in your book.
UnderstandBand 4

2. Explain how memory cells provide long-term immunity. Use the concepts of primary and secondary immune responses in your answer. 4 MARKS

Answer in your book.
ApplyBand 5

3. Some vaccines require booster shots years after the initial vaccination. Explain why this might be necessary, using your knowledge of antibodies and memory cells. 4 MARKS

Answer in your book.

Revisit Your Thinking

Go back to your Think First answer. Has your understanding changed?

Update your thinking in your book.

Answers

MCQ 1

C — B cells produce antibodies. When activated by an antigen, B cells multiply and differentiate into plasma cells that secrete antibodies.

MCQ 2

B — An antigen is a substance on the surface of a pathogen that is recognised by the immune system and triggers an immune response.

MCQ 3

B — Memory B and T cells remain after the primary response. When the same pathogen is encountered again, these memory cells enable a much faster and stronger secondary response.

MCQ 4

C — T cells directly kill infected body cells, which is essential for fighting viruses that hide inside cells where antibodies cannot reach.

MCQ 5

B — The third line of defence is specific (targets particular pathogens) and delayed (takes 5-10 days to develop fully during a primary infection).

Short Answer 1

Model answer: The second and third lines of defence differ in several ways. Speed: The second line acts immediately — inflammation, phagocytes, and fever begin within minutes to hours. The third line takes 5-10 days to reach full strength during a primary infection. Specificity: The second line is non-specific — it attacks all pathogens the same way. The third line is specific — B cells and T cells produce responses tailored to particular antigens. Cells involved: The second line uses neutrophils, macrophages, and complement proteins. The third line uses B cells (which produce antibodies), T cells (which kill infected cells), and memory cells. The second line contains and slows infection; the third line eliminates specific pathogens and provides lasting immunity.

Short Answer 2

Model answer: Memory cells provide long-term immunity by enabling a much faster and stronger response upon re-exposure to a pathogen. During the primary immune response (first infection), it takes 5-10 days for B cells and T cells to become fully activated. You may feel sick during this time. After the infection is cleared, some activated lymphocytes become memory B cells and memory T cells that persist for years or decades. If the same pathogen is encountered again, the secondary immune response begins within 1-3 days and produces 100-1,000 times more antibodies. The pathogen is usually eliminated before symptoms develop. This is the basis of long-term immunity to diseases like measles and chickenpox.

Short Answer 3

Model answer: Booster shots are necessary because antibody levels and memory cell numbers can decline over time after initial vaccination. While memory cells persist for years, their numbers may decrease gradually. A booster shot re-exposes the immune system to the antigen, reactivating memory B and T cells. This triggers a rapid secondary immune response, producing a fresh surge of antibodies and replenishing the memory cell pool. Some pathogens (like tetanus) produce toxins so dangerous that very high antibody levels are needed for protection, making boosters essential. Other vaccines (like hepatitis B) may need boosters because initial antibody responses wane faster than natural infection-induced immunity. Boosters ensure that protection remains strong enough to prevent disease.

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Lesson Game

Lymphocyte Wars

Train B cells and T cells to recognise and destroy specific pathogens! Build memory immunity and defend against repeat attacks.

Mark lesson as complete

Tick when you have finished all activities and checked your answers.